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	Primary structure and functional expression of a novel non-selective cation channel., Suzuki M., Biochem Biophys Res Commun. January 6, 1998; 242 (1): 191-6.
	Phentolamine block of KATP channels is mediated by Kir6.2., Proks P., Proc Natl Acad Sci U S A. October 14, 1997; 94 (21): 11716-20.
	The interaction of nucleotides with the tolbutamide block of cloned ATP-sensitive K+ channel currents expressed in Xenopus oocytes: a reinterpretation., Gribble FM., J Physiol. October 1, 1997; 504 ( Pt 1) 35-45.
	Activation and inhibition of K-ATP currents by guanine nucleotides is mediated by different channel subunits., Trapp S., Proc Natl Acad Sci U S A. August 5, 1997; 94 (16): 8872-7.
	Functional characterization of the transactivation properties of the PDX-1 homeodomain protein., Peshavaria M., Mol Cell Biol. July 1, 1997; 17 (7): 3987-96.
	Properties of cloned ATP-sensitive K+ currents expressed in Xenopus oocytes., Gribble FM., J Physiol. January 1, 1997; 498 ( Pt 1) 87-98.
	PACAP/VIP receptors in pancreatic beta-cells: their roles in insulin secretion., Inagaki N., Ann N Y Acad Sci. December 26, 1996; 805 44-51; discussion 52-3.
	Sequence variations in the human Kir6.2 gene, a subunit of the beta-cell ATP-sensitive K-channel: no association with NIDDM in while Caucasian subjects or evidence of abnormal function when expressed in vitro., Sakura H., Diabetologia. October 1, 1996; 39 (10): 1233-6.
	Pancreatic islet cells express a family of inwardly rectifying K+ channel subunits which interact to form G-protein-activated channels., Ferrer J., J Biol Chem. November 3, 1995; 270 (44): 26086-91.
	Two regions of GLUT 2 glucose transporter protein are responsible for its distinctive affinity for glucose., Buchs A., Endocrinology. October 1, 1995; 136 (10): 4224-30.
	Cloning and functional expression of the cDNA encoding an inwardly-rectifying potassium channel expressed in pancreatic beta-cells and in the brain., Bond CT., FEBS Lett. June 19, 1995; 367 (1): 61-6.
	Expression of murine STF-1, a putative insulin gene transcription factor, in beta cells of pancreas, duodenal epithelium and pancreatic exocrine and endocrine progenitors during ontogeny., Guz Y., Development. January 1, 1995; 121 (1): 11-8.
	Coexpression of glucose transporters and glucokinase in Xenopus oocytes indicates that both glucose transport and phosphorylation determine glucose utilization., Morita H., J Clin Invest. October 1, 1994; 94 (4): 1373-82.
	A mutation in the Glut2 glucose transporter gene of a diabetic patient abolishes transport activity., Mueckler M., J Biol Chem. July 8, 1994; 269 (27): 17765-7.
	Coupling of glucose transport and phosphorylation in Xenopus oocytes and cultured cells: determination of the rate-limiting step., Whitesell RR., J Cell Physiol. December 1, 1993; 157 (3): 509-18.
	Two nonallelic insulin genes in Xenopus laevis are expressed differentially during neurulation in prepancreatic embryos., Shuldiner AR., Proc Natl Acad Sci U S A. September 1, 1991; 88 (17): 7679-83.
	Expression of K channels in Xenopus laevis oocytes injected with poly(A+) mRNA from the insulin-secreting beta-cell line, HIT T15., Ashcroft FM., FEBS Lett. November 7, 1988; 239 (2): 185-9.

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